Nucleic acids encoding a novel neutrophil chemotactic factor

ABSTRACT

An isolated, synthetic preparation of a novel neutrophil-specific chemotactic factor (NCF), monoclonal antibodies having specific binding affinity of NCF and a clone containing the complete cDNA coding sequence for NCF are disclosed.

This is a divisional of application Ser. No. 07/169,033 filed Mar. 16, 1988 now U.S. Pat. No. 5,652,338.

BACKGROUND OF THE INVENTION

1. Technical Field

The present invention relates to an isolated, synthetic preparation of a novel neutrophil-specific chemotactic factor (NCF), monoclonal antibodies having specific binding affinity for NCF and a clone containing the complete coding sequence for NCF.

2. State of the Art

Activated monocytes/macrophages produce various mediators that cause inflammation. Among them are chemotactic factors which cause white blood cells to migrate into inflammatory sites where these factors are released. Neutrophils, the dominant leukocytes attracted by the chemotactic factors, are believed to play a critical role in the inflammatory reactions. Such diseases as rheumatoid arthritis, idiopathic pulmonary fibrosis and certain pathological inflammatory changes in many other conditions are believed to be caused by neutrophils and/or their products. However, a specific pro-inflammatory mediator released by tissue macrophages and other cells in response to inflammatory stimuli and leading to neutrophil-rich leukocyte accumulation in host defense and disease, has not heretofore been identified and isolated.

SUMMARY OF THE INVENTION

It is, therefore, an object of the present invention to provide a biologically active novel synthetic polypeptide acting as a neutrophil-specific chemotactic factor (NCF).

It is a further object of the present invention to provide a molecular clone containing the complete coding sequence for the synthesis of NCF by either prokaryotic or eukaryotic expression vectors.

It is a still further object of the present invention to provide monoclonal antibodies having specific binding affinity for NCF of the present invention.

It is another object of the present invention to provide a kit comprising a container containing the cDNA for NCF quantitation, detection or localization of NCF mRNA in a body sample.

It is yet another object of the present invention to provide a kit comprising a container containing anti-NCF antibodies having specific binding affinity for NCF for quantitation, detection or localization of NCF in a body sample.

Other objects and advantages will become evident from the following detailed description of the invention.

BRIEF DESCRIPTION OF THE DRAWINGS

These and other objects, features and many of the attendant advantages of the invention will be better understood upon a reading of the following detailed description when considered in connection with the accompanying drawings wherein:

FIG. 1 demonstrates translation of cDNA into NCF protein in reticulocyte lysate system; and

FIGS. 2a-2 d shows:

(a) Northern blot analysis of mRNA induction in lipopolysaccharide (LPS) stimulated peripheral blood mononuclear cells (PBMC);

(b) The time course of the accumulation of neutrophil chemotactic activity in culture media of PBMC after stimulation with LPS;

(c) Induction of NCF mRNA in PBMC by IL-1 or TNF, but not by IL-2, gamma-IFN, and alpha-IFN;

(d) HPLC gel filtration analysis of IL-1 and TNF induced neutrophil chemotactic activity.

DETAILED DESCRIPTION OF THE INVENTION

The above and various other objects and advantages of the present invention are achieved by a homogeneously pure, isolated, synthetic neutrophil chemotactic protein, designated herein NCF, composed in the whole or in part only of the following amino acid sequence (single letter code):

NH₂-S-A-K-E-L-R-C-Q-C-I-K-T-Y-S-K-P-F-H-P-K-F-I-K-E-L-R-V-I—E-S-G-P-H-C-A-N-T-E-I-I-V-K-L-S-D-G-R-E-L-C-L-D-P-K-E-N-W—V-Q-R-V-V-E-K-F-L-K-R-A-E-N-S.

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Although any methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, the preferred methods and materials are now described. All publications mentioned hereunder are incorporated herein by reference. Unless mentioned otherwise, the techniques employed herein are standard methodologies well known to one of ordinary skill in the art.

Chemical synthesis of the NCF of the present invention composed of the 72 amino acid residues as shown above, is achieved by commercially available polypeptide synthesizers. Alternatively, the NCF of the present invention is synthesized by standard techniques employing an expression vector containing in its genome the cloned complete coding sequence of NCF. Anti-NCF monoclonal antibodies of the present invention are prepared by standard hybridoma technology and utilized for purification and assaying purposes following standard immunological methodologies well known in the art.

High performance liquid chromatography (HPLC), in situ hybridization assays, Northern blotting analysis and the like are typical examples of the standard conventional techniques well known to one or ordinary skill in the art, which can be employed for isolation, localization, differentiation, detection, or measurement of the mRNA for NCF in biological samples.

It should be noted that the fact that chemically synthesized polypeptide of the present invention at 10 nanomolar concentrations acts as a neutrophil attracting factor, is shown by the results presented in Table 1.

TABLE 1 Chemotactic response of human neutrophils to chemically synthesized NCF. Percentage of assay Concentration of neutrophils that NCF, nanomolar migrated 1000 23 100 34 10 32 1 5 0.1 1 Hanks medium 0.3 10-⁷M fMet-Leu-Phe 40

1. It is typical for chemotactic dose-response curves to show an optimum, with a decreased response at concentrations above the optimum.

2. fMet-Leu-Phe is a commonly used reference chemoattractant.

It may be pointed out that various stimuli cause the release or secretion of more than one chemoattractant. Without the cDNA of the present invention, it is clear, of course, that the presence, specifically of the mRNA for NCF as an involved factor in a particular clinico-pathological situation, could not be definitively identified and diagnosed. cDNA of the present invention due to its binding affinity for mRNA for NCF, for the first time makes it possible to analyze body samples such as joint fluid, sputum, alveolar lavage fluid, tissue samples and the like to detect the presence or absence of mRNA for NCF. Of course, the antibodies can also be utilized for diagnostic purposes to detect the NCF and to neutralize the NCF for alleviating any disease or anomalous conditions in which the presence of NCF is found to be a causative factor.

A pharmaceutical composition for use in treating inflammatory condition comprises an anti-inflammatory effective amount of the anti-NCF monoclonal antibodies in pharmaceutically acceptable carrier, such as physiological saline, sterile non-toxic buffer and the like.

A deposit of cDNA for NCF and of the hybridoma for anti-NCF monoclonal antibodies have been made at the ATCC, Manassas, Va. on Jan. 12, 1988 and Feb. 17, 1988, respectively, under the accession numbers 40412 and HB9647, respectively. The deposits shall be viably maintained, replacing if they became non-viable, for a period of 30 years from the date of the deposit, or for 5 years from the last data of request for a sample of the deposit, whichever is longer, and made available to the public without restriction in accordance with the provisions of the law. The Commissioner of Patents and Trademarks, upon request, shall have access to the deposits.

It is understood that the examples and embodiments described herein are for illustrative purposes only and that various modifications or changes in light thereof will be suggested to persons skilled in the art and are to be included within the spirit and purview of this application and scope of the appended claims.

1 1560 BASE PAIRS NUCLEIC ACID UNKNOWN UNKNOWN 1 CTCCATAAGG CACAAACTTT CAGAGACAGC AGAGCACACA 40 AGCTTCTAGG ACAAGAGCCA GGAAGAAACC ACCGGAAGGA 80 ACCATCTCAC TGTGTGTAAA CATGACTTCC AAGCTGGCCG 120 TGGCTCTCTT GGCAGCCTTC CTGATTTCTG CAGCTCTGTG 160 TGAAGGTGCA GTTTTGCCAA GG AGT GCT AAA GAA CTT 197 AGA TGT CAG TGC ATA AAG ACA TAC TCC AAA CCT TTC 233 CAC CCC AAA TTT ATC AAA GAA CTG AGA GTG ATT GAG 269 AGT GGA CCA CAC TGC GCC AAC ACA GAA ATT ATT GTA 305 AAG CTT TCT GAT GGA AGA GAG CTC TGT CTG GAC CCC 341 AAG GAA AAC TGG GTG CAG AGG GTT GTG GAG AAG TTT 377 TTG AAG AGG GCT GAG AAT TCA TAAAAAAATT CATTCTCTGT 418 GGTATCCAAG AATCAGTGAA GATGCCAGTG AAACTTCAAG 458 CAAATCTACT TCAACACTTC ATGTATTGTG TGGGTCTGTT 498 GTAGGGTTGC CAGATGCAAT ACAAGATTCC TGGTTAAATT 538 TGAATTTCAG TAAACAATGA ATAGTTTTTC ATTGTACCAT 578 GAAATATCCA GAACATACTT ATATGTAAAG TATTATTTAT 618 TTGAATCTAC AAAAAACAAC AAATAATTTT TAAATATAAG 658 GATTTTCCTA GATATTGCAC GGGAGAATAT ACAAATAGCA 698 AAATTGGGCC AAGGGCCAAG AGAATATCCG AACTTTAATT 738 TCAGGAATTG AATGGGTTTG CTAGAATGTG ATATTTGAAG 778 CATCACATAA AAATGATGGG ACAATAAATT TTGCCATAAA 818 GTCAAATTTA GCTGGAAATC CTGGATTTTT TTCTGTTAAA 858 TCTGGCAACC CTAGTCTGCT AGCCAGGATC CACAAGTCCT 898 TGTTCCACTG TGCCTTGGTT TCTCCTTTAT TTCTAAGTGG 938 AAAAAGTATT AGCCACCATC TTACCTCACA GTGATGTTGT 978 GAGGACATGT GGAAGCACTT TAAGTTTTTT CATCATAACA 1018 TAAATTATTT TCAAGTGTAA CTTATTAACC TATTTATTAT 1058 TTATGTATTT ATTTAAGCAT CAAATATTTG TGCAAGAATT 1098 TGGAAAAATA GAAGATGAAT CATTGATTGA ATAGTTATAA 1138 AGATGTTATA GTAAATTTAT TTTATTTTAG ATATTAAATG 1178 ATGTTTTATT AGATAAATTT CAATCAGGGT TTTTAGATTA 1218 AACAAACAAA CAATTGGGTA CCCAGTTAAA TTTTCATTTC 1258 AGATATACAA CAAATAATTT TTTAGTATAA GTACATTATT 1298 GTTTATCTGA AATTTTAATT GAACTAACAA TCCTAGTTTG 1338 ATACTCCCAG TCTTGTCATT GCCAGCTGTG TTGGTAGTGC 1378 TGTGTTGAAT TACGGAATAA TGAGTTAGAA CTATTAAAAC 1418 AGCCAAAACT CCACAGTCAA TATTAGTAAT TTCTTGCTGG 1458 TTGAAACTTG TTTATTATGT ACAAATAGAT TCTTATAATA 1498 TTATTTAAAT GACTGCATTT TTAAATACAA GGCTTTATAT 1538 TTTTAACTTT AAAAAAAACC GG 1560 

What is claimed is:
 1. A nucleic acid molecule encoding a neutrophil chemotactic factor polypeptide having an amino acid sequence represented by the single letter code: NH₂-S-A-K-E-L-R-C-Q-C-I-K-T-Y-S-K-P-F-H-P-K-F-I-K-E-L-R—V-I-E-S-G-P-H-C-A-N-T-E-I-I-V-K-L-S-D-G-R-E-L-C-L-D-L-P-K—E-N-W-V-Q-R-V-V-E-K-F-L-K-R-A-E-N-S.
 2. A recombinant expression vector comprising the nucleic acid molecule of claim
 1. 3. The nucleic acid molecule of claim 1, wherein said molecule has the sequence shown from positions 183 to 398 in SEQ ID NO:1.
 4. A recombinant expression vector comprising the nucleic acid molecule of claim
 3. 5. The nucleic acid molecule of claim 1, wherein said molecule has ATCC accession number
 40412. 6. A recombinant expression vector comprising the nucleic acid molecule of claim
 5. 